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GM2 gangliosidosis, variant B or Tay-Sachs disease is marked by accumulation of G2 gangliosides due to hexosaminidase A deficiency
|Subclass of|| lysosomal storage disease,|
eye degenerative disease
|Discoverer or inventor|| |
This category has the following 2 subcategories, out of 2 total.
Media in category "Tay–Sachs disease"
The following 6 files are in this category, out of 6 total.